# FDA Inspection 1116146 - FujiFilm Ultra Pure Solutions, Inc. - January 15, 2020

Source: https://www.globalkeysolutions.net/records/fda_inspections/fujifilm-ultra-pure-solutions-inc/98933305-da5c-4e48-8f9f-c607b90c8524
Source feed: FDA_Inspections

> FDA Inspection 1116146 for FujiFilm Ultra Pure Solutions, Inc. on January 15, 2020. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1116146
- Company Name: FujiFilm Ultra Pure Solutions, Inc.
- Inspection Date: 2020-01-15
- Classification: No Action Indicated (NAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

## Related Documents

- [FDA Inspection 996404 - 2017-01-12](https://www.globalkeysolutions.net/records/fda_inspections/fujifilm-ultra-pure-solutions-inc/7882f518-e6a7-4848-afea-06a662f35a0a)
- [FDA Inspection 678306 - 2010-09-01](https://www.globalkeysolutions.net/records/fda_inspections/fujifilm-ultra-pure-solutions-inc/d9aed843-d32e-4618-a51f-d639cdf6532c)

Company: https://www.globalkeysolutions.net/companies/fujifilm-ultra-pure-solutions-inc/958bdfeb-69bc-412d-b79e-2cfcb8615ef6

Office: https://www.globalkeysolutions.net/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c
